Theaflavin Compositions, Related Processes and Methods of Use

ABSTRACT

A process for producing purified theaflavin extract is provided which comprises combining an organic solvent with tea leaves, extracting polyphenols from the tea leaves to produce an organic stock substrate solution; producing a second batch of tea leaves; grinding the second batch of tea leaves to produce stock fermentation enzyme; combining the stock substrate solution with the stock fermentation enzyme to produce a fermentation mixture; fermentation of the mixture to produce theaflavins; and, separating the theaflavins from the fermentation mixture to produce purified theaflavin extract. Oral dosage forms are provided which comprise an effective amount of the purified theaflavin extract. Methods of treatment of human physiological disorders are provided which comprise administering an oral dosage form.

FIELD OF THE INVENTION

The present invention relates to processes for production of purifiedtheaflavin extract, compositions which result from the processes, oraldosage forms, and methods of use.

BACKGROUND OF THE INVENTION

Theaflavin (catechin dimer joined at B rings) and its derivatives, knowncollectively as theaflavins, are antioxidant polyphenols Flavan-3-olsformed from catechins during enzymatic oxidation (fermentation).Theaflavins generally comprise a mixture of theaflavin,theaflavin-3-gallate, theaflavin-3′-gallate andtheaflavin-3,3′-digallate.

Theaflavins have positive health benefits directly linked to theantioxidant properties of these compounds. The benefits include theability to effect lower blood lipid levels (e.g. cholesterol), controlof inflammation, as well as anti-tumor effects. See, e.g., Maron D J, etal., Cholesterol-Lowering Effect of a Theaflavin-Enriched Green TeaExtract: a Randomized Controlled Trial, Arch. Intern. Med. 163 (12):1448 (2003). See, also, Lorentz, M., et al., Basic Res Cardiol. 2009January; 104(1):100; Manna, S., et al., J Nutr Biochem. 2009 May;20(5):337.

Limited availability of theaflavins, economically derived from naturalsources, however, presents a significant barrier to realization of thehealth benefits of theaflavins. Commercial reagents such as polyphenolperoxidase and hydrogen peroxide from commercial sources are often usedin the fermentation step, which further increases the cost of theproduction. Goodsall, et al., U.S. Pat. Nos. 6,833,144; 6,113,965. Manycurrent extraction and purification steps employ environmentallyunfriendly solvents methanol and chloroform. Environmental hazardsmoreover result from current processes due to the frequent applicationof strong acids and bases and large amounts of resulting wastegenerated.

An ongoing need for low cost, high yield, environmentally friendlyscalable production of theaflavins from natural sources indeed existstoward realization of numerous health benefits.

SUMMARY OF THE INVENTION

A process for producing purified theaflavin extract is provided whichcomprises combining an organic solvent with tea leaves, extractingpolyphenols from the tea leaves to produce an organic stock substratesolution; producing a second batch of tea leaves; grinding the secondbatch of tea leaves to produce stock fermentation enzyme; combining thestock substrate solution with the stock fermentation enzyme to produce afermentation mixture; fermentation of the mixture to producetheaflavins; and,

separating the theaflavins from the fermentation mixture to producepurified theaflavin extract.

In addition, the current invention is directed to Oral dosage formswhich comprise an effective amount of the purified theaflavin extract.

The invention is further directed to methods of treatment of humanphysiological disorders are provided which comprise administering anoral dosage form.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 displays a process embodiment of the present invention formanufacturing theaflavins.

DETAILED DESCRIPTION OF THE INVENTION

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as is commonly understood by one of skill in theart to which this invention belongs. All publications and patentsreferred to herein are incorporated by reference including U.S. Pat.Nos. 7,427,622; 7,157,493 and 7,288,680.

As used herein the term organic solvent refers to any inert organicsolvent that solubilizes tea leaf polyphenols including but not limitedto esters, alcohols, ketones and ethers. The term inert as used hereinrefers to an organic solvent that does not otherwise affect theoxidation of polyphenols to theaflavins in the processes describedherein. Esters for use as organic solvent in processes described hereininclude, but are not limited to, for example, methyl acetate, ethylacetate, propyl acetate, and isopropyl acetate. Alcohols for use asorganic solvent in processes described herein include, but are notlimited to, for example, ethyl alcohol, propyl alcohol, and isopropylalcohol. Ketones for use as organic solvent in processes describedherein include, but are not limited to, for example, acetone andbutanone. Ethers for use as organic solvent in processes describedherein include, but are not limited to, for example, diethyl ether,dipropyl ether, and methyl-tert-butyl ether.

The term organic stock substrate solution, as used herein, refers to anorganic tea leaf extract containing polyphenols.

The term stock fermentation enzyme, as used herein, refers to a sourceof endogenous enzymes in tea leaves, polyphenol oxidase (PO) andpolyphenol peroxidase (PPO) for example.

The term fermentation mixture, as used herein, refers to an organic tealeaf extract containing polyphenols mixed with endogenous enzymes in tealeaves and wherein the polyphenols undergo oxidation to flavins by meansof the enzymes including polyphenol oxidase (PO) and polyphenolperoxidase (PPO).

The term water, as used herein has its ordinary meaning, but includesacidic aqueous and basic aqueous.

The term human physiological disorder as used herein refers toinflammation and related disease, including but not limited to,hyperlipidemia, coronary heart disease, apoplexy, arthescleroticcardiovascular diseases, AIDS, diabetes, oxidated-low densitylipoprotein level, von Willebrand's disease, leukopenia, cerebralinfarction, dementia and physical disorder, and fatty liver.

The term oral dosage form as used herein includes but is not limited toa tablet, capsule, powder, solution, suspension, emulsion, pill, pellet,sustained-release formulation that contain an effective amount oftheaflavins produced by methods according to the present invention.However, since theaflavins produced by methods according to the presentinvention are incorporated into food items such as nutritional bars andnutritional drinks the term oral dosage form includes food and drinkitems that incorporate an effective amount of theaflavins produced bymethods according to the present invention.

As used herein the term theaflavins includes but is not limited totheaflavin, isotheaflavin, neotheaflavin, theaflavin-3-gallate,theaflavin-3′-gallate, theaflavin-3,3′-digallate, epitheaflavic acid,epitheaflavic acid-3′-gallate, theaflavic acid, theaflavicacid-3′-gallate and mixtures thereof. The term includes salt forms ofthese compounds.

Fermentation refers to an oxidative process to produce theaflavins, andoptionally thearubigins.

Fermentation enzyme refers to the native reagents of tea leaves whicheffect fermentation. Preferably whole tea leaves optionally treated witha solvent, preferably moisturized with aqueous solution, pure water or0.05%-1% of citric acid solution, for example, frozen, and then ground,preferably to particles, for example, smaller than about 100 mesh.

The term “washing” refers to a process of mixing thoroughly an organicphase with an aqueous phase, separating the organic phase from theaqueous phase, and collecting the organic phase. Optionally, thisprocess can be repeated one or more times and the organic phases arecombined.

Solute transferring refers to a process of adding an aqueous phase to anorganic phase to form a mixture, concentrating said mixture and forcingthe solute in the organic phase to be transferred into the aqueousphase.

This present invention provides an improved process for economicmanufacture of high quality theaflavins wherein tea polyphenols areextracted into an organic solvent and oxidized, for example, in theorganic solvent by means of native enzymes directly from tea leafmaterial without using other source of polyphenols. The fermentationprocess takes place in an organic phase, which not only improves theyield of theaflavins at low cost, but avoids problems such as emulsionsin other manufacturing processes in multiphase media. Processembodiments of the present invention employ, for example, neutral orweakly acidic conditions.

An improved process for manufacturing theaflavins is describedcomprising the steps of extracting preferably green tea leaves with anorganic solvent to produce an organic stock substrate solution,preparing stock fermentation enzyme from tea leaves, and fermenting theorganic stock substrate solution with the stock fermentation enzyme, forexample, in an oxygenated environment to produce a fermentation mixture.Embodiments of the process described herein include filtering theresulting fermentation mixture and concentrating the resulting filtrate.Embodiments include washing the filtrate with an aqueous solution, thenadding water to the washed filtrate and concentrating the resultingaqueous phase to produce aqueous theaflavin extract by removing,evaporating for example, remaining organic solvent. Embodiments includefiltration of the aqueous theaflavin extract to remove insolubleimpurities at this point to produce purified aqueous theaflavin extract.Embodiments include lyophilization or spray drying of the purifiedaqueous theaflavin extract to produce solid purified theaflavin extract.Example solid purified theaflavin extract compositions produce by theprocesses described herein contain about 45% theaflavins. Treatment ofhuman physiological disorders are provided which comprise administeringan effective amount of purified theaflavin extracts described herein.Oral dosage forms are provided which comprise an effective amount ofpurified theaflavin extracts described herein.

Example Theaflavin Extract Characteristics Resulting from NovelProcesses:

TABLE I characteristics Appearance and result Note Pale yellow to redbrown color, astringent theaflavin ≧40.0 HPLC analysis method content %Water content % ≦6.0 Ash content % ≦2.0 Heavy metal (ppm) ≦10 arsenic(ppm) ≦2 caffeine % ≦4

The present invention has a number of advantages over traditionalprocesses. Because the fermentation process takes place in an organicphase and tea leaves, homogenized for example, are used as the source offermentation enzyme, the manufacturing process is readily controllableand avoids problems such as emulsifications in traditional processes. Inaddition, this low cost manufacturing process produces theaflavins inhigh quality with a theaflavin content of up to 45% by weight determinedby HPLC. The caffeine level, for example, is reduced to about 4% orless. The solubility, taste, and color of the product are significantlyimproved. Processes described herein, without using toxic solvent orgenerating large amount of waste, are environmentally friendly. Organicsolvent is recycled, for example. Neutral or weakly acidic aqueousconditions are employed, for example, to enhance the quality of theproduct.

An exemplary embodiment process of the present invention includes but isnot limited to, for example:

-   -   a. Preparation of fermentation stock solution (extracting of        green leaves with an organic solvent): 500 Kg, for example,        Green tea leaves are added into an extractor (Multifunctional        Dynamic Extracting Tank; Model: ZY-DTQ-6.0; Manufacturer:        Wenzhou Zhongyuan Light Industry Machine Co., for example),        followed by the addition of 5000 Kg, for example, ethyl acetate.        The mixture is stirred and extracted for 10-120 minutes, for        example, at 10° C.-90° C., for example. The organic phase is        collected. A second portion of 5000 Kg, for example, ethyl        acetate is used for extracting the green tea leaves. The organic        phases are combined, and concentrated at 0.06 Mpa, for example,        at below 80° C., for example, (Scraped Evaporator, Model:        ZYE-40; Manufacturer: Changshu Pharmaceutical & Chemical        Equipment General Factory, for example) until a solid content of        between about 0.5% and about 5% is reached; then cooled to room        temperature and used as the fermentation stock solution.    -   b. Preparation of fermentation enzyme: Fresh tea leaves 600 Kg,        for example, are moisturized using pure water or 0.01%-1%, for        example, of citric acid solution, frozen, and ground (40-100        Mesh, for example) as the fermentation enzyme.    -   c. Fermentation: 5000 L, for example, of fermentation stock        solution obtained from step (a) is added to a fermentor (Model:        FXG; Manufacturer: Changshu Pharmaceutical & Chemical Equipment        General Factory, for example), followed by the addition of 500        Kg, for example, fermentation enzyme from step (b). The mixture        in the fermentor undergoes fermentation process in the presence        of gas, e.g., air with an agitation at 20° C.-60° C., for        example. The air flow rate is controlled at range of, for        example, 0.2-40 m³/min, agitation speed, for example, 30-150        rpm. The ratio of fermentation stock solution and the enzyme by        weight, for example, is between about 5:1 to about 40:1.    -   d. Separation: The fermentation solution from the step (c) is        filtered through, for example, 120 mesh filter screen and        divided into filtrate and filter residue.    -   e. Concentration: The filtrate from the step (d) is        concentrated, for example, using Scraped Evaporator under        conditions, for example, of relative vacuum 0.06 Mpa and        temperature preferably below 80° C. (Model: ZYE-40;        Manufacturer: Changshu Pharmaceutical & Chemical Equipment        General Factory, for example) to solid content, for example, of        5%-30%.    -   f. Washing: The concentrated filtrate from the step (e) is put        into water scrubber (Washing Vessel, Model: SX1000,        Manufacturer: Changshu Pharmaceutical & Chemical Equipment        General Factory, for example) and then the acidic solution is        added. The mixture is stirred up and then allowed to stand to        separate into two layers. The bottom aqueous layer is removed.        The remaining organic phase is washed 1-20 times using the same        method as above. The ratio of the acidic solution and        concentrate by volume is about 0.1:1-20:1, for example. After        washing, the organic phase and aqueous phase are collected,        respectively. The aqueous phase is concentrated and dried to        form the by-product. The organic phase is used in step.    -   g. Solute transferring: Pure water is added into the organic        phase solution obtained from the above step (f). The ratio of        pure water and organic phase solution is bout 1:1-1:50 by        weight, for example. The organic phase and water are mixed        thoroughly and concentrated at controlled temperature.    -   h. Filtration: The concentrate obtained from step (g) is cooled        to 10° C.-60° C., for example, and filtered. The filtrate is        collected.    -   i. Concentrating and freeze-drying: The filtrate obtained from        the step (h) is further concentrated to solid content of        15%-80%, for example, by using High Efficiency Rotary Scraped        Evaporator (Model: DN1200; Manufacturer: Wuxi Xuelang        Fermentation Equipment Co., Ltd.) at relative vacuum 0.085 Mpa,        for example, and temperature below 80° C., for example. The        concentrate is subjected to spray drying, or lyophilization,        then ground using high speed mill, for example, and screened        using screen grader, for example, to obtain the product of        theaflavins.

Exemplary modifications of processes of the present invention,exemplified a-i, supra, include embodiments wherein the ratio of tealeaves, preferably green tea, and ethyl acetate each time in step (a)above for the preparation of fermentation stock solution is within therange of about 1:10 to about 1:30. The example process of preparation ofenzyme in step (b) is performed at below 0° C., for example, betweenabout −10° C. and 0° C., for at least about 2 hours. The size of groundfresh tea leaves is preferably about 80 mesh or smaller. Gas introducedinto the fermentation process in step (c) is preferably pure oxygen. Thetemperatures in the concentration (step (e)) and transferring solute(step (g)) are controlled at below 80° C., for example between about 60°C. and about 80° C.]. The acidic solution added in washing process instep (f) is about 0.05% to about 1% of aqueous citric acid. Thetemperatures of the lyophilization process for concentration in step (i)are preferably controlled at below about −35° C. to form an ice block.The vacuum level is preferably about 0.6-1 mmHg while water vapor isevaporated from the ice block. The temperature is then increased, forexample, at a rate of 1-5° C./hour to 0° C., then, for example, at arate of 1-10° C. to 25° C.-30° C. and stayed, for example, for 1-4 hoursuntil the water content of the product reaches about 3% to about 5%, forexample. The vacuum is removed to obtain, for example, a theaflavinsproduct of the present invention.

Preferred embodiment processes of the present invention are wherein thecontrolled temperature is between 25-60° C., for example, for extractinggreen tea leaves. A further example is wherein the fermentation stocksolution and said fermentation enzyme are in a ratio of about 5:1 toabout 20:1 by weight. Another example process feature is wherein saidsecond controlled temperature is between 20-40° C. Solid product may beobtained by means of spray drying or lyophilization, for example.

Preparation of Fermentation Stock Solution (Organic Stock SubstrateSolution) for Fermentation Enzymatic Oxidation:

To a container, green tea leaves, preferably shredded into 5-60 mesh,are added, followed by the addition of ethyl acetate. The ratio of greentea leaves and ethyl acetate added is between about 1:5 and about 1:30by weight, for example. The mixture is stirred and extracted for 10-120minutes, for example, at 10° C.-90° C., for example. The extractedsolution is collected by filtration or decantation. To the resultingsolid residue ethyl acetate is added. The ratio of solid residue andethyl acetate at this point is between about 1:5 and about 1:30 byweight, for example. The extraction procedure is repeated to yield asecond extraction. Extracted ethyl acetate solutions, for example, arecombined to one container, concentrated at vacuum 0.085-0.054 Mpa at56-80° C. in a rotating evaporator (e.g., model: RE-200, Shanghai KexingInstrument Co.) to solid content in the range of 0.5%-5%, and cooled toroom temperature as the fermentation stock solution (organic stocksubstrate solution).

Preparation of fermentation Enzyme (stock fermentation enzyme), e.g.,Polyphenol oxidase and polyphenol peroxidase: Fresh tea leaves aremoistened with pure water or 0.01%-1% of citric acid aqueous solution,for example, frozen for at least about 2 hours, for example, then groundand filtered through a screen, preferably of at least about 80 mesh,resulting in an example stock fermentation enzyme.

Fermentation process: The fermentation stock solution (organic stocksubstrate solution) is added to a fermentor (fermentation container),followed by the addition of the fermentation enzyme (stock fermentationenzyme). A preferred ratio of fermentation stock solution and the enzymeis between about 5:1 and about 40:1 by weight. Gas, preferably pureoxygen, is introduced into the resulting mixture in the fermentor whilestirred at about 30- to about 150 rpm, for example. The fermentation(enzymatic oxidation) is preferred to proceed at about 20° C. to about60° C.

Separation: The fermentation solution mixture is separated (theaflavinsfrom the fermentation mixture to produce purified theaflavin extract) byfiltration, for example, and divided into filtrate and solid residue.

Concentration: The filtrate (theaflavin extract) is concentrated on arotating evaporator (e.g. rotating evaporator (Model: RE-200,Manufacturer: Shanghai Kexing Instrument Co.) at controlled temperatureto yield a mixture with about 5% to about 30% solid content.

Washing: Concentrated mixture is transferred to a water scrubber (e.g.,Pear Shaped Separatory Funnel, 500 ml, Manufacturer: Shanghai ShendiGlassware Co.) followed by acidic solution, preferably 0.05%-1% citricacid aqueous solution. The ratio of the acidic solution and concentratedmixture by volume is between about 0.1:1 and about 20:1, for example.The two phases (aqueous and organic) are mixed thoroughly and wereallowed to stand to separate. The bottom layer, i.e., water layer, isremoved. The remained top layer is washed 1-20 times using the samemethod, i.e. addition of acidic solution while being stirred and mixed,separation of two layers and removal of the bottom water layer. Theratio of the acidic solution and concentrate by volume is about 0.1:1 toabout 10:1, for example. After washing, the organic phase and aqueousphase are collected, respectively. The aqueous phase is concentrated anddried to form the product. The organic phase is further processed.

Pure water is added to the organic solution obtained. The ratio of purewater and ester organic phase solution is between about 1:1 and about1:50 by weight, for example. This is concentrated at controlledtemperature, preferably at or below 80° C.

Filtration: the concentrate solution obtained from step G is cooled to10° C.-60° C., for example, then filtered. The filtrate is collected.

Concentration and Drying: Filtrate obtained from step (h) is furtherconcentrated to the solid content of 15%-80%. The resulting concentrateis dried by lyophilization, or spray drying, ground, and screened toobtain product theaflavins.

Preferred features of the process described herein include temperaturesof the concentration/lyophilization is controlled at −35° C. or below,the vacuum level is about 0.6-1 mmHg. The water vapor is evaporated fromthe ice block particles of theaflavins concentrate, then, thetemperature is increased at the rate of 1-5° C./hour to 0° C., then thetemperature is increased at the rate of 1-10° C. to 25° C.-30° C.,keeping for 1-4 hours, for example, until the water content of theproduct reaches to 3%-5%, and finally, the vacuum is released.

“Treating” or “treatment” of any disease or disorder refers, in oneembodiment, to ameliorating the disease or disorder (i.e., arresting orreducing the development of the disease or at least one of the clinicalsymptoms thereof). In another embodiment “treating” or “treatment”refers to ameliorating at least one physical parameter, which may not bediscernible by the patient. In yet another embodiment, “treating” or“treatment” refers to inhibiting the disease or disorder, eitherphysically, (e.g., stabilization of a discernible symptom),physiologically, (e.g., stabilization of a physical parameter), or both.In yet another embodiment, “treating” or “treatment” refers to delayingthe onset of the disease or disorder.

“Therapeutically effective amount” means the amount of a compound that,when administered to a patient for treating or preventing a disease, issufficient to effect such treatment or prevention of the disease. The“therapeutically effective amount” will vary depending on the diseaseand its severity and the age, weight, etc., of the patient to betreated.

Further, in certain embodiments, compounds of the invention and/orpharmaceutical compositions thereof are administered to a patient,preferably a human, as a preventative measure against the above diseasesor conditions. Thus, the theaflavins of the invention and/orcompositions thereof may be administered as a preventative measure to apatient having a predisposition for any of the above diseases ordisorders. Accordingly, the theaflavins of the invention and/orpharmaceutical compositions thereof may be used for the treating orpreventing one disease or disorder and concurrently treating orpreventing another (e.g., preventing hyperlipidemia while treating acerebral infarction).

The suitability of the theaflavins of the invention and/or compositionsthereof in treating or preventing the various diseases or disorderslisted above may be determined by methods described in the art.Accordingly, it is well within the capability of those of skill in theart to assay and use the compounds of the invention and/orpharmaceutical compositions thereof to treat or prevent the abovediseases or disorders.

Therapeutic/Prophylactic Administration

The theaflavins of the invention and/or compositions thereof may beadvantageously used in human and veterinary medicine.

When used to treat or prevent the above diseases or disorders,theaflavins of the invention and/or compositions thereof may beadministered or applied singly, or in combination with other agents. Thecompounds of the invention and/or pharmaceutical compositions thereofmay also be administered or applied singly, in combination with otherpharmaceutically active agents including other compounds of theinvention and/or pharmaceutical compositions thereof.

The current invention provides methods of treatment and prophylaxis byadministration to a patient of a therapeutically effective amount of acompound of the invention and/or pharmaceutical composition thereof. Thepatient is preferably a mammal and most preferably, is a human.

The compounds of the invention and/or pharmaceutical compositionsthereof are preferably administered orally, which results in the releaseof the compounds of the invention and/or pharmaceutical compositionsthereof into the bloodstream. The compounds of the invention and/orpharmaceutical compositions thereof can be delivered via oral sustainedrelease systems. In one embodiment, polymeric materials are used fororal sustained release delivery. Preferred polymers include sodiumcarboxymethylcellulose, hydroxypropylcellulose,hydroxypropylmethylcellulose and hydroxyethylcellulose (most preferred,hydroxypropyl methylcellulose). Other preferred cellulose ethers havebeen described (Alderman, Int. J. Pharm. Tech. & Prod. Mfr. 1984, 5(3)1-9). Factors affecting drug release are well known to the skilledartisan and have been described in the art (Bamba et al., Int. J. Pharm.1979, 2, 307).

In another embodiment, enteric-coated preparations can be used for oralsustained release administration. Preferred coating materials includepolymers with a pH-dependent solubility (i.e., pH-controlled release),polymers with a slow or pH-dependent rate of swelling, dissolution orerosion (i.e., time-controlled release), polymers that are degraded byenzymes (i.e., enzyme-controlled release) and polymers that form firmlayers that are destroyed by an increase in pressure (i.e.,pressure-controlled release).

In still another embodiment, osmotic delivery systems are used for oralsustained release administration (Verma et al., Drug Dev. Ind. Pharm.,2000, 26:695-708). In still another embodiment, OROS™ osmotic devicesare used for oral sustained release delivery devices (Theeuwes et al.,U.S. Pat. No. 3,845,770; Theeuwes et al., U.S. Pat. No. 3,916,899).

In one embodiment, the compounds of the invention are encapsulated fororal administration. Preferably, encapsulation protects the compounds ofthe invention from light and/or oxygen degradation. The capsulepreferably, is comprised of a shell and a fill material, where eitherthe shell or fill material contains an radiation blocker and/or ananti-oxidant.

The shell material is comprised of a gelling agent, water and optionallya plasticizer. Accordingly, the shell material may form either a hardgel or a soft gel. The gelling agent may be, but is not limited to,gelatin, modified starch, carrageenan, gellan, mannan gum, amylose,xanthan, alginates, agar, guar, gum arabic, pectin, cyclodextrin orcombination thereof. The shell may optionally include an emulsifier,thickener, preservative, flavoring, sweetener, colorant, radiationblocker, opacifying agent, anti-oxidant, masticatory substance, etc.

Gelatin, as is well known in the art, is manufactured by the hydrolysisof animal by-products such as bones, skin, and connective tissue whichcontain collagen. Bovine animals and pigs are the primary sources ofgelatin

Modified starches, include, for example, non-retrograding starchesderived by chemical modification of starch from any plant source such ascorn, waxy maize, potato, wheat, rice, tapioca, sorghum, etc. Usefulmodified starches are ether and ester derivatives of starch including,for example, hydroxypropyl, hydroxyethyl, succinate, and octenylsuccinate starch derivatives. Other modified starches which may be usedinclude the thermally converted, fluidity or thin boiling type productsderived from the above chemically modified starches. These materials maybe of lower molecular weight, prepared by heating the modified starch,subjecting the starch to hydrolytic acid and/or heat treatment, etc.

Carrageenan is a natural sulfated polysaccharide hydrocolloid derivedfrom seaweed, and is a mixture of galactose and 3-6-anhydrogalactosecopolymers. A number of different carrageenan types exist (e.g., kappa,iota, lambda, etc.) and it is anticipated that any of these may be usedin the present invention.

Gellan gum is an extracellular polysaccharide obtained by aerobicfermentation of the microorganism, Pseudomonas elodea. Various forms ofgellum gum including, but not limited to, native, deacetylated,deacylated clarified, partially deacetylated, partially deacylatedclarified may be sued in the present invention.

Mannam gum include the galactomannan gums, the glucomannan gums andmixtures thereof. Accordingly, mannam gum includes, but is not limitedto, locust bean gum, konjac gum, tara gum and cassia gum.

In some embodiments, a gelling salt may be used in the presentinvention. Accordingly, a calcium salt, a magnesium salt, a barium salt,a sodium salt or a potassium salt of an appropriate inorganic or organicacid may be used to form the shell of a capsule of the presentinvention.

Plasticizers are preferably, polyols, such as, for example, glycerin,sorbitol, an alkylene glycol, maltitol, lactitol, xylitol, corn syrupsolids, etc. and combinations thereof. In one embodiment, theplasticizer is a combination of glycerin and sorbitol.

In another embodiment, the capsule shell comprises between about 10% and90% gelatin, and between about 5% and about 40% water. In anotherembodiment, the capsule shell comprises between about 10% and 90%gelatin, between about 1% and about 30% plasticizer and between about 5%and about 40% water. In still another embodiment, the capsule shellcomprises between about 25 to about 45% gelatin, between about 1% andabout 30% plasticizer and between about 5% and about 40% water. In stillanother embodiment, the capsule shell comprises between about 25 toabout 45% gelatin, between about 1% and about 30% plasticizer, betweenabout 1 and 5% radiation blocker and between about 1% and about 5%colorant and between about 5% and about 40% water.

The capsule shell of the present invention encloses a pre-selectedquantity of fill material. Preferably, the enclosed fill material willcontain a therapeutically effective amount of a mixture of theaflavins.The fill material may be a liquid, a semi-solid, a solid and gel.

The fill material may include a pharmaceutically acceptable vehicle,which may be prepared by a number of diverse methods which are known tothose of skill in the art. The pharmaceutically acceptable vehicle mustbe compatible with the capsule shell and preferably, does not degradethe capsule shell during a period of typical storage. Solutions to theabove problem are well known to the skilled artisan.

Suitable liquid pharmaceutically acceptable vehicles for the fillmaterial include, but are not limited to, neutral oil, mineral oil,water, alcohol, polyalkylene glycol, vegetable oil and fructose syrup.Preferably, the liquid pharmaceutically acceptable vehicle is avegetable oil, more preferably, a corn oil, peanut oil, safflower oil,sunflower oil and soybean oil and most preferably soybean oil. Theliquid pharmaceutically acceptable vehicle may include an emulsifier,thickener, preservative, flavoring, sweetener, colorant, radiationblocker, opacifying agent, anti-oxidant, masticatory substance, etc.

The present capsules may also include a solid fill material. Usefulsolid fill materials include, but are not limited to, tablets or pelletscomprising the mixture of theaflavins, which may be further coated withgelatin, sugar, etc. (Glassman, U.S. Pat. No. 3,228,789). The tablets orpellets may contain co-solvents, buffers, emulsifiers, thickeners,preservatives, sweeteners, flavorings, colorants, radiation blockers,anti-oxidants, opacifying agent, masticatory substances, etc.

The present capsules may also include a semi-solid fill material. Themixture of theaflavins may, for example, be dispersed in a substantiallywater-free carrier mixture comprising one or more polyalkylene glycols,preferably, comprising a mixture of liquid polyalkylene glycol and waxypolyalkylene glycol and in minor amount a C2-C.sub.4 diol or triol (Shahet al., U.S. Pat. No. 4,935,243). A flavoring, preservative, sweetener,colorant, radiation blocker, co-solvent, buffer, emulsifier, thickener,anti-oxidant, opacifying agent, masticatory substance, etc., may beadded to the semi-solid fill material.

The present capsules may also enclose a gel fill comprising a gelledpolymeric matrix, which may be generated by gelling a liquid fillfollowed by encapsulation (Cohen et al, U.S. Pat. No. 4,708,834). Thegelled fill may comprise a solution or dispersion of an activeingredient in a polysaccharide gum and may also optionally, includeco-solvents, preservative, buffers, emulsifiers, thickeners, sweeteners,flavorings, colorant, radiation blocker, opacifying agent, anti-oxidant,masticatory substance, etc.

Masticatory substances, for example, include, but are not limited to,Chicle, Chiquibul, Crown gum, Gutta hang kang, Massaranduba balata,Massaranduba chocolate, Nispero, Leche caspi, Pendare, Perillo, Leche devac, Niger gutta, Tunu, Chite and Natural rubber. Flavorings include,but are not limited to, cherry syrup, citric acid, dextrose, essentialoil, vanillin, cinnamon oil, orange oil, spearmint oil, strawberry oil,nutmeg oil. A preferred stiffener is beeswax while a preferredemulsifier is lecithin. Other stiffeners and emulsifiers which may beuseful in the present invention are known to the skilled artisan.Preferred anti-oxidants include ascorbic acid and vitamin E.

In one embodiment, the fill material comprises between about 1% andabout 20% mixture of theaflavins, between about 1% and about 5%anti-oxidant, between about 5% and about 90% pharmaceutically acceptablecarrier, between about 1% and about 20% emulsifier; and between about 1%to about 20% stiffening agent.

Oral Dosage Compositions

The present oral dosage compositions typically contain a therapeuticallyeffective amount of a compound of the invention, preferably in purifiedform, together with a suitable amount of a pharmaceutically acceptablevehicle, so as to provide the form for proper administration to apatient. The compounds of the invention may be present at a level ofbetween about 5% and about 50% (w/w), preferably, about 11% in apharmaceutical composition, for example. Total amount of the compound ofthe invention per dose may be between about 70 mg and about 210 mg.

When administered to a patient, the compounds of the invention andpharmaceutically acceptable vehicle are preferably sterile. Water,saline solutions and aqueous dextrose and glycerol solutions may beemployed as liquid vehicles. Other suitable pharmaceutical vehiclesinclude excipients such as starch, glucose, lactose, sucrose, gelatin,malt, rice, flour, chalk, silica gel, sodium stearate, glycerolmonostearate, talc, sodium chloride, dried skim milk, glycerol,propylene, glycol, water, ethanol and the like. The presentpharmaceutical compositions, if desired, can also contain minor amountsof wetting or emu 1 sifying agents or pH buffering agents. In addition,auxiliary, stabilizing, thickening, lubricating and coloring agents maybe used. A general discussion of the preparation of pharmaceuticalcompositions may be found in Remington, “The Science and Practice ofPharmacy,” 19th Edition.

Pharmaceutical compositions comprising a compound of the invention maybe manufactured by means of conventional mixing, dissolving,granulating, dragee-making, levigating, emulsifying, encapsulating,entrapping or lyophilizing processes. Pharmaceutical compositions may beformulated in conventional manner using one or more physiologicallyacceptable carriers, diluents, excipients or auxiliaries, whichfacilitate processing of compounds of the invention into preparationswhich can be used pharmaceutically.

The present pharmaceutical compositions can take the form of solutions,suspensions, emulsion, tablets, pills, pellets, capsules, capsulescontaining liquids, powders, sustained-release formulations, emulsionsor any other form suitable for oral use. In one embodiment, thepharmaceutically acceptable vehicle is a capsule (see e.g., Grosswald etal., U.S. Pat. No. 5,698,155). Other examples of suitable pharmaceuticalvehicles have been described in the art (see Remington, “The Science andPractice of Pharmacy,” 19th Edition, 1995). Orally administeredpharmaceutical compositions may contain one or more optional agents, forexample, sweetening agents such as fructose, aspartame or saccharin;flavoring agents such as peppermint, oil of wintergreen, or cherrycoloring agents and preserving agents, to provide a pharmaceuticallypalatable preparation. Moreover, when in tablet or pill form, thepharmaceutical compositions may be coated to delay disintegration andabsorption in the gastrointestinal tract, thereby providing a sustainedaction over an extended period of time. Selectively permeable membranessurrounding an osmotically active driving compound are also suitable fororally administered compounds of the invention. In these laterplatforms, fluid from the environment surrounding the capsule is imbibedby the driving compound, which swells to displace the agent or agentcomposition through an aperture. These delivery platforms can provide anessentially zero order delivery profile as opposed to the spikedprofiles of immediate release formulations. A time delay material suchas glycerol monostearate or glycerol stearate may also be used. Oralcompositions can include standard vehicles such as mannitol, lactose,starch, magnesium stearate, sodium saccharine, cellulose, magnesiumcarbonate, etc. Such vehicles are preferably of pharmaceutical grade.

For oral liquid preparations such as, for example, suspensions, elixirsand solutions, suitable carriers, excipients or diluents include water,saline, alkyleneglycols (e.g., propylene glycol), polyalkylene glycols(e.g., polyethylene glycol) oils, alcohols, slightly acidic buffersbetween pH 4 and pH 6 (e.g., acetate, citrate, ascorbate at betweenabout 5.0 mM to about 50.0 mM), etc. Additionally, flavoring agents,preservatives, coloring agents, bile salts, acylcamitines and the likemay be added. For buccal administration, the pharmaceutical compositionsmay take the form of tablets, lozenges, etc. formulated in conventionalmanner.

When a compound of the invention is acidic or basic, it may be includedin any of the above-described formulations as the free acid or freebase, a pharmaceutically acceptable salt, a solvate or hydrate.Pharmaceutically acceptable salts substantially retain the activity ofthe free acid or base, may be prepared by reaction with bases or acidsand tend to be more soluble in aqueous and other protic solvents thanthe corresponding free acid or base form.

Therapeutic Doses

Theaflavins of the invention and/or pharmaceutical composition thereof,will generally be used in an amount effective to achieve the intendedpurpose. For use to treat or prevent diseases or disorders the compoundsof the invention and/or pharmaceutical compositions thereof, areadministered or applied in a therapeutically effective amount.

The amount of a compound of the invention and/or pharmaceuticalcomposition thereof that will be effective in the treatment of aparticular disorder or condition disclosed herein will depend on thenature of the disorder or condition, and can be determined by standardclinical techniques known in the art and by doctors skilled in treatingor preventing a particular disease or disorder. In addition, in vitro orin vivo assays may optionally be employed to help identify optimaldosage ranges. The amount of a compound of the invention and/orpharmaceutical composition thereof administered will, of course, bedependent on, among other factors, the subject being treated, the weightof the subject, the severity of the affliction, the manner ofadministration and the judgment of the prescribing physician.

For example, the dosage may be delivered in a pharmaceutical compositionby a single administration, by multiple applications or controlledrelease. In one embodiment, the compounds of the invention are deliveredby oral sustained release administration. Preferably, in thisembodiment, the compounds of the invention are administered twice perday (more preferably, once per day). Dosing may be repeatedintermittently, may be provided alone or in combination with other drugsand may continue as long as required for effective treatment of thedisease state or disorder.

Suitable dosage ranges for oral administration are dependent on thenature of the compounds of the invention administered (e.g., whether thetheaflavins are administered together or whether theaflavin,theaflavin-3-gallate, theaflavin-3′-gallate or theaflavin-3,3′-digallateare administered, each as a separate compound) but are generally about0.001 mg to about 200 mg of a compound of the invention per kilogrambody weight. In one embodiment, the dosage range is between about 0.1mg/kg to about 5 mg/kg. Dosage ranges may be readily determined bymethods known to the artisan of ordinary skill. Effective doses may beextrapolated from dose-response curves derived from in vitro or animalmodel test systems. Such animal models and systems are well-known in theart.

The compounds of the invention are preferably assayed in vitro and invivo, for the desired therapeutic or prophylactic activity, prior to usein humans. For example, in vitro assays can be used to determine whetheradministration of a specific compound of the invention or a combinationof compounds of the invention is preferred. The compounds of theinvention may also be demonstrated to be effective and safe using animalmodel systems.

Preferably, a therapeutically effective dose of a compound of theinvention and/or pharmaceutical composition thereof described hereinwill provide therapeutic benefit without causing substantial toxicity.Toxicity of compounds of the invention and/or pharmaceuticalcompositions thereof may be determined using standard pharmaceuticalprocedures and may be readily ascertained by the skilled artisan. Thedose ratio between toxic and therapeutic effect is the therapeuticindex. A compound of the invention and/or pharmaceutical compositionthereof will preferably exhibit particularly high therapeutic indices intreating disease and disorders. The dosage of a compound of theinvention and/or pharmaceutical composition thereof described hereinwill preferably be within a range of circulating concentrations thatinclude an effective dose with little or no toxicity.

Combination Therapy

In certain embodiments of the present invention, the compounds of theinvention and/or pharmaceutical compositions thereof can be used incombination therapy with at least one other therapeutic agent. Thecompound of the invention and/or pharmaceutical composition thereof andthe therapeutic agent can act additively or, more preferably,synergistically. In a preferred embodiment, a compound of the inventionand/or a pharmaceutical composition thereof is administered concurrentlywith the administration of another therapeutic agent. In anotherembodiment, a compound of the invention and/or pharmaceuticalcomposition thereof is administered prior or subsequent toadministration of another therapeutic agent.

In particular, in one preferred embodiment, the compounds of theinvention and/or pharmaceutical compositions thereof can be used incombination therapy with other agents used to treat or preventhyperlipidemia, coronary heart disease, apoplexy, arthescleroticcardiovascular diseases, AIDS, diabetes, oxidated-low densitylipoprotein level, von Willebrand's disease, leukopenia, cerebralinfarction, dementia and physical disorder and fatty liver.

Diet Supplement Compositions

The present diet supplement compositions typically contain one or morecompounds of the invention, preferably in purified form, together with asuitable amount of a diet supplement vehicle, so as to provide the formfor proper administration to a user.

There are many types of nutrition bars and other “snack” bars availableon the market, and many consumers use such products as a convenient foodsource. For example, grain based bars such as granola bars are easy tocarry and provide a healthy, good tasting food that is consumed byactive people such as hikers and athletes, and by everybody else.Because grain-based nutrition bars are convenient and healthy, they havebecome a very popular product.

One type of bar that has become popular in the recent years is commonlycalled an “energy bar” or “performance bar.” U.S. Pat. No. 7,247,336,for example is herein incorporated by reference. U.S. Pat. No.6,143,335, McKenzie, R. G., for example, teaches scoring a food bar intobite-sized pieces thus providing a method for delivering exactquantities of supplemental ingredients to animals or humans. Theseproducts are typically especially formulated for use by activeindividuals such as athletes, and include ingredients that are intendedto boost athletic performance, endurance, etc. Such energy bars providean easy way for athletes to consume foods that are especially formulatedto improve performance.

EXAMPLES Example I

See, FIG. 1. (1) To an example extraction container (2000 ml electricstirring device, flask with three-neck, condensing tube and waterbath.), 100 g of green tea was added, followed by the addition of 1000ml ethyl acetate. The temperature was controlled at a range of 25°C.-60° C. Thus formed mixture was stirred at speed of 30-150 rpm for 30min. The liquid layer (or extraction solution) was then collected. Tothe solid residue, another 1000 ml of ethyl acetate was added. Theextraction process was repeated. The extracted solution was combined andconcentrated at vacuum −0.085 Mpa and 70° C. in a rotating evaporator(Model: RE-200, Manufacturer: Shanghai Kexing Instrument Co.), to asuspension that contains approximate 1% (w/v) of the solid. Thesuspension was then cooled to ambient temperature and thus formed thefermentation stock solution. (2) The starting enzyme was prepared from120 g of fresh tea leaves. The fresh tea leaves were sprinkled with purewater or a 0.05-1% citric acid aqueous solution, then cooled to 0° C. orbelow and frozen for a minimum of 2 hours. The frozen tea leaves werecrushed to small particles of about 80 mesh at a room temperature. Thusprepared enzyme materials were ready to use (storing time is less than 2hours at ambient temperature). (3) To a fermentation container (glassreactor, Model: DAT serial, Manufacturer: Shanghai Kexing InstrumentCo.), 1000 g of fermentation stock solution prepared from step (1) and100 g of enzyme materials prepared in step (2) were added and oxygen wasintroduced at flow rate of 600 ml/min, while the mixture was stirred at30-150 rpm at 20-60° C. Analytical samples were collected from thefermentation container at each 30 min for a total time of 4-8 hoursdepending on the actual analytical results. When the reaction wascomplete, both oxygen flow and stirring were stopped. The end point ofthe reaction is determined by a curve of time-absorption value preparedat 380 nm, e.g. when the absorption value for theaflavins is steady astime increases, the end point is considered to be reached. (4)Immediately after the reaction was stopped, the reaction mixture wasfiltered through a 120 mesh filter screen. Both the filtrate and thesolid residue were collected. The solid residue was treated and thendried as a byproduct. The filtrate was concentrated at emperature of60-80° C. and vacuum of −0.085 Mpa or above, by using rotatingevaporator (Model: RE-200, Manufacturer: Shanghai Kexing InstrumentCo.). When the solid content in the solution reached 8% (w/v), theconcentrated solution was transferred to a washing container (Pear ShapeSeparatory Funnel, 500 ml, Manufacturer: Shanghai Shendi Glassware Co.).The concentrated solution (ethyl acetate solution) was washed with 0.05%citric acid aqueous solution. The volume of washing solution is equal to20% of the concentrated solution, and the ethyl acetate solution waswashed 8 times. Both the organic layer and the aqueous layer werecollected. The combined aqueous layer was concentrated and dried toyield byproducts. To the organic layer (ethyl acetate layer), 100 mlwater was added and the resulted mixture was further concentrated at60-80° C. till the substantially complete removal of ethyl acetate. Theaqueous layer (theaflavins solution) was then collected and cooled to40° C. The solution was filtered through a 120 mesh filter screen toremove insoluble impurities. The filtrate was collected and concentratedat about 60-80° C. and vacuum of −0.085 Mpa or above to solid content of40% (w/v). The concentrator used in above steps is a rotating evaporator(Model: RE-200, Manufacturer: shanghai Kexing Instrument Co., Ltd.). Theresulted mixture was cooled to −35° C., then lyophilized under a vacuumof 0.6-1 mmHg. Upon the removal of the ice chunk or ice particles andunder the same vacuum condition, the temperature of the solid productwas increased gradually to 0° C. at a controlled rate at 3° C./hour,then to 25-30° C. at a controlled rate of 5° C./hour. After the solidproduct was dried under the same vacuum and 25-30° C. for 1-2 hours andthe water content reached 3%-5% in the solid product, the vacuum wasreleased and the solid product was crushed by a micro high speed mill(Model: XA-1, Particle Size: 80-150 mesh, Manufacturer: Jiangyan YinheInstrument Co. Ltd.) and screened through a screen grader to give 6.2 gof theaflavins product. Analysis of the product showed the theaflavinscontent of 46.2%. (w/w)

Example II

A process of manufacturing theaflavins: (1) As shown in Figure I, to anextraction container (2000 ml, specially designed and assembled byinventors, which is consisted of electric stirring device, flask withthree-neck, condensing tube and water bath.), 100 g of green tea wasadded, followed by the addition of 1500 ml ethyl acetate. Thetemperature was controlled at a range of 20° C.-40° C. Thus formedmixture was stirred at speed of 30-150 rpm for 30 min. The organic phase(or extraction solution) was collected. To the solid residue, another1500 ml of ethyl acetate was added and the above extraction process wasrepeated. The extracted organic phases were combined and concentrated atvacuum −0.085 Mpa and 70° C. in a rotating evaporator (Model: RE-200,Manufacturer: Shanghai Kexing Instrument Co., Ltd.) to a suspension thatcontains approximately 0.8% (w/v) of solid. The suspension was thencooled to ambient temperature and thus formed the fermentation stocksolution. (2) The starting fermentation enzyme was prepared from 180 gof fresh tea leaves. The fresh tea leaves were sprinkled with pure wateror a citric acid aqueous solution (0.5%), then cooled to 0° C. or belowand frozen for a minimum of 2 hours. The frozen tea leaves were crashedto small particles of 80 mesh below room temperature. Thus preparedfermentation enzyme was ready to use (storing time is less than 2 hoursat ambient temperature). (3) To a fermentation container (glass reactor,Model: DAT serial, Manufacturer: Shanghai Kexing Instrument Co., Ltd),1500 g of fermentation stock solution prepared from step (1) and 150 gof fermentation enzyme materials prepared in step (2) were added andoxygen was introduced at flow rate of 600 ml/min while the mixture wasstirred at 30-150 rpm at 20-25° C. Analytical samples were collectedfrom the fermentation container every 30 min for a total time of 4-8hours depending on the actual analytical results. Both oxygen flow andstirring were stopped, and thus the process was stopped completely. Theend point of the reaction is determined by a curve of time-absorptionvalue prepared at 380 nm, e.g. when the absorption value for theaflavinsis steady as time increases, the end point is considered to be reached.(4) Immediately after the reaction was stopped, the reaction mixture wasfiltered through a 120 mesh filter screen. Both the filtrate and thesolid residue were collected. The solid residue was treated and thendried as a byproduct. The filtrate was concentrated at temperature of60-80° C. and vacuum of −0.085 Mpa or above, by using rotatingevaporator (Model: RE-200. Manufacturer: Shanghai Kexing Instrument Co.,Ltd.). When the solid content in the solution reached 8% (w/v), theconcentrated solution was transferred to a washing container (Pear ShapeSeparatory Funnel, 500 ml, Manufacturer: Shanghai Shendi Glassware Co.,Ltd.). The concentrated solution (ethyl acetate solution) was washedwith 0.05% citric acid aqueous solution. The volume of washing solutionis equal to 10% of the concentrated solution and the ethyl acetatesolution was washed 8 times. Both the organic layer and the aqueouslayer were collected. The combined aqueous layer was concentrated anddried to yield byproducts. To the organic layer (ethyl acetate layer),140 ml of water was added and the resulting mixture was furtherconcentrated at 80° C. or below till the complete removal of ethylacetate. The aqueous layer (theaflavin solution) was then collected andcooled to 40° C. The solution was filtered through a 100 mesh filterscreen to remove insoluble impurities. The filtrate was collected andconcentrated at about 60-80° C. and vacuum of −0.085 Mpa or above tosolid content of 40% (w/v). The concentrator used in above steps is arotating evaporator (Model: RE-200, Manufacturer: shanghai KexingInstrument Co., Ltd.). The resulted mixture was cooled to −35° C., thenlyophilized under a vacuum of 0.6-1 mmHg. Upon the removal of the icechunk or ice particles and under the same vacuum condition, thetemperature of the solid product was increased gradually to 0° C. at acontrolled rate at 3° C./hour, then to 25-30° C. at a controlled rate of5° C./hour. After the solid product was dried under the same vacuum at25-30° C. for 1-2 hours and the water content reached 3%-5% in the solidproduct, the vacuum was removed. The solid product was crashed by amicro high speed mill (Model: XA-1, Particle Size: 80-150 mesh,Manufacturer: Jiangyan Yinhe Instrument Co., Ltd.) and screened througha screen grader to give 6.4 g of theaflavin product. Analysis of theproduct showed a theaflavin content of 45.8% (w/w).

Example III

A process of manufacturing theaflavins: (1) As shown in FIG. 1, to anextraction container (5000 ml, specially designed and assembled byinventors, which is consisted of electric stirring device, flask withthree-neck, condensing tube and water bath.), 100 g of green tea wasadded, followed by the addition of 3000 ml ethyl acetate. Thetemperature was controlled at a range of 25° C.-60° C. Thus formedmixture was stirred and extracted at speed of 30-150 rpm for 30 min. Theorganic phase (or extraction solution) was collected. To the solidresidue, another 3000 ml of ethyl acetate was added and the aboveextraction process was repeated. The extracted organic phases werecombined and concentrated at vacuum 0.085 Mpa and 70° C. in a rotatingevaporator (Model: RE-200, Manufacturer: Shanghai Kexing Instrument Co.,Ltd.), to a suspension that contains approximately 0.5% of solid (w/v).The suspension was then cooled to ambient temperature and thus formedthe fermentation stock solution. (2) The fermentation enzyme wasprepared from 180 g of fresh tea leaves. The fresh tea leaves weresprinkled with pure water or a citric acid aqueous solution (1%), thencooled to 0° C. or below and frozen for a minimum of 2 hours. The frozentea leaves were crashed to small particle size of 80 mesh below roomtemperature. Thus prepared fermentation enzyme was ready to use (storingtime is less than 2 hours at ambient temperature). (3) To a fermentationcontainer (glass reactor, Model: DAT serial, Manufacturer: ShanghaiKexing Instrument Co., Ltd), 3000 g of felt tentation stock solutionprepared from step (1) and 150 g of enzyme materials prepared in step(2) were added and oxygen was introduced at flow rate of 600 ml/min,while the mixture was stirred at 30-150 rpm at 20° C. Analytical sampleswere collected from the fermentation container every hour till thefermentation process was essentially complete. The total period of timeof fermentation is 4-8 hours depending on the actual test results. Bothoxygen flow and stirring were stopped, and thus the process was stoppedcompletely. The end point of the reaction is determined by a curve oftime-absorption prepared at 380 nm, e.g. when the absorption value issteady as time increases, the end point is considered to be reached. (4)Immediately after the reaction was stopped, the reaction mixture wasfiltered through a 120 mesh filter screen. Both the filtrate and thesolid residue were collected. The filtrate was concentrated attemperature of 60-80° C. and vacuum of −0.085 Mpa or above, by usingrotating evaporator (Model: RE-200, Manufacturer: Shanghai KexingInstrument Co., Ltd.). When the solid content in the solution reached15% (w/v), the concentrated solution was transferred to a washingcontainer (Pear Shape Separatory Funnel, 500 ml, Manufacturer: ShanghaiShendi Glassware Co., Ltd.). The concentrated solution (ethyl acetatesolution) was washed with 1% citric acid aqueous solution. The ethylacetate solution was washed 8 times. Both the organic layer and theaqueous layer were collected. The combined aqueous layer wasconcentrated and dried to yield byproducts. To the organic layer (ethylacetate layer), 50 ml water was added and the resulted mixture wasfurther concentrated at 80° C. till the complete removal of ethylacetate. The aqueous layer (theaflavins solution) was then collected andcooled to 30° C. The solution was filtered through a 100 mesh filterscreen to remove insoluble impurities. The filtrate was collected andconcentrated at about 70° C. and vacuum of −0.085 Mpa or above in arotating evaporator (Model: RE-200, Manufacturer: shanghai KexingInstrument Co., Ltd.) to solid content of 25% (w/v). The resultedmixture was cooled to −35° C., then lyophilized under a vacuum of 0.6-1mmHg. Upon the removal of the ice chunk or ice particles and under thesame vacuum condition, the temperature of the solid product wasincreased gradually to 0° C. at a controlled rate at 3° C./hour, then to25-30° C. at a controlled rate of 5° C./hour. After the solid productwas dried under the same vacuum at 25-30° C. for 1-2 hours and the watercontent reached 3%-5% in the solid product, the vacuum was removed andthe solid product was crashed by a micro high speed mill (Model: XA-1,Particle Size: 80-150 mesh, Manufacturer: Jiangyan Yinhe Instrument Co.,Ltd.) and screened through a screen grader to give 6.3 g of theaflavinsproduct. Analysis of the product showed a theaflavins content of 46.1%(w/w).

Example IV

A process of manufacturing theaflavins: (1) As shown in Figure I, to anextraction container (2000 ml, specially designed and assembled byinventors, which is consisted of electric stirring device, flask withthree-neck, condensing tube and water bath.), 100 g of green tea wasadded, followed by the addition of 1000 ml ethyl acetate. Thetemperature was controlled at a range of 25-60° C. Thus formed mixturewas stirred and extracted at speed of 100-150 rpm for 30 min. The liquidlayer (or extraction solution) was collected. To the solid residue,another 1000 ml of ethyl acetate was added and the above extractionprocess was repeated. The extracted solution was combined andconcentrated at 60-80° C. and vacuum of −0.085 Mpa orrr above in arotating evaporator (Model: RE-200, Manufacturer: Shanghai KexingInstrument Co., Ltd.), to a suspension that contains approximate 1% ofsolid (w/v). The suspension was then cooled to ambient temperature andthus formed the fermentation stock solution. (2) The fermentation enzymewas prepared from 220 g of fresh tea leaves. The fresh tea leaves weresprinkled with pure water or a citric acid aqueous solution (0.1%), thencooled to 0° C. or below and frozen for a minimum of 2 hours. The frozentea leaves were crashed to small particle size of 80 mesh below roomtemperature. Thus prepared fermentation enzyme was ready to use (storingtime is less than 2 hours at ambient temperature). (3) To a fermentationcontainer (glass reactor, Model: DAT serial, Manufacturer: ShanghaiKexing Instrument Co., Ltd), 1000 g of fermentation stock solutionprepared from step (1) and 200 g of fermentation enzyme prepared in step(2) was added and oxygen was introduced at flow rate of 600 ml/min,while the mixture was stirred at 30-150 rpm at 20° C. Analytical sampleswere collected from the fermentation container every hour till thefermentation process was essentially complete. The total period of timeof fermentation is 4-8 hours depending on the actual analytical results.Both oxygen flow and stirring were stopped, and thus the process wasstopped completely. The end point of the reaction is determined by acurve of time-absorption prepared at 380 nm, e.g. when the absorptionvalue is steady as time increases, the end point is considered to bereached. (4) Immediately after the reaction was stopped, the reactionmixture was filtered through a filter screen. Both the filtrate and thesolid residue were collected. The filtrate was concentrated attemperature of 60-80° C. and vacuum of −0.085 Mpa or above, by usingrotating evaporator (Model: RE-200, Manufacturer: Shanghai KexingInstrument Co., Ltd.). When the solid content in the solution reached 8%(w/v), the concentrated solution was transferred to a washing container(Pear Shape Separatory Funnel, 500 ml, Manufacturer: Shanghai ShendiGlassware Co. Ltd.). The concentrated solution (ethyl acetate solution)was washed with 0.1% citric acid aqueous solution. The volume of washingsolution is equal to 20% of the concentrated solution, and the ethylacetate solution was washed 8 times. Both the organic layer and theaqueous layer were collected. The combined aqueous layer wasconcentrated and dried to yield byproducts. To the organic layer (ethylacetate layer), 100 ml water was added and the resulted mixture wasfurther concentrated at 60-80° C. till the complete removal of ethylacetate. The aqueous layer (theaflavins solution) was then collected andcooled to 60° C. The solution was filtered through a 100 mesh filterscreen to remove insoluble impurities. The filtrate was collected andconcentrated at about 70° C. and vacuum of −0.085 Mpa or above to solidcontent of 80% (w/v). The concentrator used in above steps is a rotatingevaporator (Model: RE-200, Manufacturer: shanghai Kexing Instrument Co.,Ltd.) The resulting mixture was cooled to −35° C., then lyophilizedunder a vacuum of 0.6-1 mmHg. Upon the removal of the ice chunk or iceparticles and under the same vacuum condition, the temperature of thesolid product was increased gradually to 0° C. at a controlled rate at3° C./hour, then to 25-30° C. at a controlled rate of 5° C./hour. Afterthe solid product was dried under the same vacuum at 25-30° C. for 1-2hours and the water content reached 3%-5% in the solid product, thevacuum was removed and the solid product was crashed by a micro highspeed mill (Model: XA-1, Particle Size: 80-150 mesh, Manufacturer:Jiangyan Yinhe Instrument Co., Ltd.) and screened through a screengrader to give 6.2 g of theaflavins product. Analysis of the productshowed a theaflavins content of 47.8% (w/w).

Example V

A process of manufacturing theaflavins: (1) As shown in Figure I, to anextraction container (3000 ml, specially designed and assembled byinventors, which is consisted of electric stirring device, flask withthree-neck, condensing tube and water bath.), 200 g of green tea wasadded, followed by the addition of 2000 ml ethyl acetate. Thetemperature was controlled at a range of 25° C.-60° C. Thus formedmixture was stirred and extracted at speed of 30-150 rpm for 30 min. Theliquid layer (or extraction solution) was collected. To the solidresidue, another 2000 ml of ethyl acetate was added and the aboveextraction process was repeated once. The extracted solution wascombined and concentrated at vacuum −0.085 Mpa and 70° C. in a rotatingevaporator (Model: RE-200, Manufacturer: Shanghai Kexing Instrument Co.,Ltd.), to a suspension that contains approximate 1% of solid (w/v). Thesuspension was then cooled to ambient temperature and thus formed thefermentation stock solution. (2) The fermentation enzyme was preparedfrom 220 g of fresh tea leaves. The fresh tea leaves were sprinkled withpure water or a citric acid aqueous solution (0.1%), then cooled to 0°C. or below and frozen for a minimum of 2 hours. The frozen tea leaveswere crashed to small particle size of 80 mesh below room temperature.Thus prepared fermentation enzyme was ready to use (storing time is lessthan 2 hours at ambient temperature). (3) To a fermentation container(glass reactor, Model: DAT serial, Manufacturer: Shanghai KexingInstrument Co., Ltd), 2000 g of fermentation stock solution preparedfrom step (1) and 200 g of fermentation enzyme prepared in step (2) wasadded and oxygen was introduced at flow rate of 600 ml/min, while themixture was stirred at 30-150 rpm at 25° C. Analytical samples werecollected from the fermentation container every hour till thefermentation process was essentially complete. Both oxygen flow andstirring were stopped, and thus the process was stopped completely. Thetotal period of time of fermentation is 4-8 hours depending on theactual test results. The end point of the reaction is determined by acurve of time-absorption prepared at 380 nm, e.g. when the absorptionvalue is steady as time increases, the end point is considered to bereached. (4) Immediately after the reaction was stopped, the reactionmixture was filtered through a 120 mesh filter screen. Both the filtrateand the solid residue were collected. The filtrate was concentrated attemperature of 60-80° C. and vacuum of −0.085 Mpa or above, by usingrotating evaporator (Model: RE-200, Manufacturer: Shanghai KexingInstrument Co., Ltd.). When the solid content in the solution reached 8%(w/v), the concentrated solution was transferred to a washing container(Pear Shape Separatory Funnel, 500 ml, Manufacturer: Shanghai ShendiGlassware Co. Ltd.). The concentrated solution (ethyl acetate solution)was washed with 0.1% citric acid aqueous solution. The volume of washingsolution is equal to 20% of the concentrated solution, and the ethylacetate solution was washed 20 times. Both the organic layer and theaqueous layer were collected. The combined aqueous layer wasconcentrated to yield byproducts. To the organic layer (ethyl acetatelayer), 100 ml water was added and the resulted mixture was furtherconcentrated at 60-80° C. till the complete removal of ethyl acetate.The aqueous layer (theaflavins solution) was then collected and cooledto 40° C. The solution was filtered through a 100 mesh filter screen toremove insoluble impurities. The filtrate was collected and concentratedat about 60-80° C. and vacuum of −0.085 Mpa or above in a rotatingevaporator (Model: RE-200, Manufacturer: shanghai Kexing Instrument Co.,Ltd.) to solid content of 40% (v). The resulted mixture was cooled to−35° C., and then lyophilized under a vacuum of 0.6-1 mmHg. Upon theremoval of the ice chunk or ice particles and under the same vacuumcondition, the temperature of the solid product was increased graduallyto 0° C. at a controlled rate at 3° C./hour, then to 25-30° C. at acontrolled rate of 5° C./hour. After the solid product was dried underthe same vacuum and 25-30° C. for 1-2 hours and the water contentreached 3%-5% in the solid product, the vacuum was removed and the solidproduct was crashed by a micro high speed mill (Model: XA-1, ParticleSize: 80-150 mesh, Manufacturer: Jiangyan Yinhe Instrument Co., Ltd.)and screened through a screen grader to give 13.12 g of theaflavinproduct. Analysis of the product showed a theaflavins content of 47%(w/w).

Example VI

A process of manufacturing theaflavins: (1) As shown in Figure I, to anextraction container (2000 ml, specially designed and assembled byinventors, which is consisted of electric stirring device, flask withthree-neck, condensing tube and water bath.), 100 g of green tea wasadded, followed by the addition of 1000 ml ethyl acetate. Thetemperature was controlled at a range of 25-60° C. Thus formed mixturewas stirred and extracted at speed of 30-150 rpm for 30 min. The liquidlayer (or extraction solution) was collected. To the solid residue,another 1000 ml of ethyl acetate was added and the above extractionprocess was repeated once. The extracted solution was combined andconcentrated at vacuum −0.085 Mpa or at 70° C. in a rotating evaporator(Model: RE-200, Manufacturer: Shanghai Kexing Instrument Co., Ltd.), toa suspension that contains approximate 1% of solid (w/v). The suspensionwas then cooled to ambient temperature and thus formed a fermentationstock solution. (2) The fermentation enzyme was prepared from 220 g offresh tea leaves. The fresh tea leaves were sprinkled with pure water ora citric acid aqueous solution (0.1%), then cooled to 0° C. or below andfrozen for a minimum of 2 hours. The frozen tea leaves were crashed tosmall particle size of 80 mesh below room temperature. Thus preparedfermentation enzyme was ready to use (storing time is not more than 2hours at ambient temperature). (3) To a fermentation container (glassreactor, Model: DAT serial, Manufacturer: Shanghai Kexing InstrumentCo., Ltd), 1000 g of fermentation stock solution prepared from step (1)and 200 g of fermentation enzyme prepared in step (2) was added andoxygen was introduced at flow rate of 600 ml/min, while the mixture wasstirred at 30-150 rpm at 25° C. Analytical samples were collected fromthe fermentation container every hour till the fermentation process wasessentially complete. Both oxygen flow and stirring were stopped, andthus the process was stopped completely. The total period of time offermentation is 4-8 hours depending on the actual test results. The endpoint of the reaction is determined by a curve of time-absorptionprepared at 380 nm, e.g. when the absorption value is steady as timeincreases, the reaction is considered to be completed. (4) Immediatelyafter the reaction was stopped, the reaction mixture was filteredthrough a 120 mesh filter screen. Both the filtrate and the solidresidue were collected. The filtrate was concentrated at temperature of60-80° C. and vacuum of −0.085 Mpa or above, by using rotatingevaporator (Model: RE-200, Manufacturer: Shanghai Kexing Instrument Co.,Ltd.). When the solid content in the solution reached 8% (w/v), theconcentrated solution was transferred to a washing container (Pear ShapeSeparatory Funnel, 500 ml, Manufacturer: Shanghai Shendi Glassware Co.,Ltd.). The concentrated solution (ethyl acetate solution) was washedwith 0.1% citric acid aqueous solution. The volume of washing solutionis equal to 20% of the concentrated solution and the ethyl acetatesolution was washed once. Both the organic layer and the aqueous layerwere collected. The combined aqueous layer was concentrated and dried toyield byproducts. To the organic layer (ethyl acetate layer), 100 mlwater was added and the resulted mixture was further concentrated at60-80° C. till the complete removal of ethyl acetate. The aqueous layer(theaflavins solution) was then collected and cooled to 60° C. Thesolution was filtered through a 100 mesh filter screen to removeinsoluble impurities. The filtrate was collected and concentrated atabout 70° C. and vacuum of −0.085 Mpa or above in a rotating evaporator(Model: RE-200, Manufacturer: shanghai Kexing Instrument Co., Ltd.) tosolid content of 50% (w/v). The resulted mixture was cooled to −35° C.,then lyophilized under a vacuum of 0.6-1 mmHg. Upon the removal of theice chunk or ice particles and under the same vacuum condition, thetemperature of the solid product was increased gradually to 0° C. at acontrolled rate at 3° C./hour, then to 25-30° C. at a controlled rate of5° C./hour. After the solid product was dried under the same vacuum and25-30° C. for 1-2 hours and the water content reached 3%-5% in the solidproduct, the vacuum was removed and the solid product was crashed by amicro high speed mill (Model: XA-1, Particle Size: 80-150 mesh,Manufacturer: Jiangyan Yinhe Instrument Co., Ltd.) and screened througha screen grader to give 6.1 g of theaflavins product. Analysis of theproduct showed a theaflavins content of 46% (w/w).

Example VII

(1) To a extraction container (2000 ml, specially designed and assembledby inventors, which is consisted of electric stirring device, flask withthree-neck, condensing tube and water bath.), 100 g of green tea wasadded, followed by the addition of 1000 ml ethyl acetate. Thetemperature was controlled at a range of 25° C.-60° C. Thus formedmixture was stirred at speed of 30-150 rpm for 30 min. The liquid layer(or extraction solution) was then collected. To the solid residue,another 1000 ml of ethyl acetate was added and the above extractionprocess was repeated. The extracted solution was combined andconcentrated at vacuum −0.085 Mpa and 70° C. in a rotating evaporator(Model: RE-200, Manufacturer: Shanghai Kexing Instrument Co., Ltd.), toa suspension that contains approximate 1% (w/v) of the solid. Thesuspension was then cooled to ambient temperature and thus formed thefermentation stock solution. (2) The starting enzyme was prepared from120 g of fresh tea leaves. The fresh tea leaves were sprinkled with purewater or a 0.1% citric acid aqueous solution, then cooled to 0° C. orbelow and frozen for a minimum of 2 hours. The frozen tea leaves werecrushed to small particles of about 80 mesh at a room temperature. Thusprepared enzyme materials were ready to use (storing time is not morethan 2 hours at ambient temperature). (3) To a fermentation container(glass reactor, Model: DAT serial, Manufacturer: Shanghai KexingInstrument Co., Ltd), 1000 g of fermentation stock solution preparedfrom step (1) and 100 g of enzyme materials prepared in step (2) wereadded and oxygen was introduced at flow rate of 600 ml/min, while themixture was stirred at 30-150 rpm at 20° C. Analytical samples werecollected from the fermentation container at each 30 min for a totaltime of 4-8 hours depending on the actual analytical results. When thereaction was complete, both oxygen flow and stirring were stopped. Theend point of the reaction is determined by a curve of time-absorptionvalue prepared at 380 nm, e.g. when the absorption value for theaflavinsis steady as time increases, the end point is considered to be reached.(4) Immediately after the reaction was stopped, the reaction mixture wasfiltered through a 120 mesh filter screen. Both the filtrate and thesolid residue were collected. The solid residue was treated and thendried as a byproduct. The filtrate was concentrated at temperature of60-80° C. and vacuum of −0.085 Mpa or above, by using rotatingevaporator (Model: RE-200, Manufacturer: Shanghai Kexing Instrument Co.,Ltd.). When the solid content in the solution reached 8% (w/v), theconcentrated solution was transferred to a washing container (Pear ShapeSeparatory Funnel, 500 ml, Manufacturer: Shanghai Shendi Glassware Co.,Ltd.). The concentrated solution (ethyl acetate solution) was washedwith 0.1% citric acid aqueous solution. The volume of washing solutionis equal to 20% of the concentrated solution, and the ethyl acetatesolution was washed 8 times. Both the organic layer and the aqueouslayer were collected. The combined aqueous layer was concentrated anddried to yield byproducts. To the organic layer (ethyl acetate layer),100 ml water was added and the resulted mixture was further concentratedat 60-80° C. till the substantially complete removal of ethyl acetate.The aqueous layer (theaflavins solution) was then collected and cooledto 40° C. The solution was filtered through a 100 mesh filter screen toremove insoluble impurities. The solution was filtered through a 100mesh filter screen to remove insoluble impurities. The filtrate wascollected and concentrated at about 60-80° C. and vacuum of −0.085 Mpaor above to solid content of 20-60% (w/v). The concentrator used inabove steps is a rotating evaporator (Model: RE-200, Manufacturer:shanghai Kexing Instrument Co., Ltd.) The concentrate was introduced tospray dryer (Model YC-015, Manufacturer: Wuxi DongshengSpray-granulating & Srying Equipment Plant) by pump. Inlet airtemperature of the spray dryer was controlled at 180-220° C., whenoutlet air temperature reached at 80-100° C., collected the driedproduct, and then screened through a screen grader to give 6.6 g oftheaflavins product. Analysis of the product showed the theaflavinscontent of 45.8%. (w/w).

All publications and patents mentioned in the above specification areherein incorporated by reference. Various modifications and variationsof the described compositions and methods of the invention will beapparent to those skilled in the art without departing from the scopeand spirit of the invention. Although the invention has been describedin connection with specific preferred embodiments, it should beunderstood that the invention as claimed should not be unduly limited tosuch specific embodiments. Indeed, various modifications of thedescribed compositions and modes for carrying out the invention whichare obvious to those skilled in the art or related fields are intendedto be within the scope of the following claims.

1.-20. (canceled)
 21. A method for treatment of a human physiologicaldisorder comprising administering to a human diagnosed with thephysiological disorder an effective amount of a product composition oftheaflavins produced by the process comprising providing a first batchof tea leaves; combining an organic solvent selected from the groupconsisting of ester, alcohol, ketone, ether, or a combination thereofwith the first batch of tea leaves; extracting polyphenols from thefirst batch of tea leaves to produce an organic stock substrate solutionof polyphenols in the organic solvent; providing a second batch of tealeaves; grinding the second batch of tea leaves to produce stockfermentation enzyme; combining the organic stock substrate solution withthe stock fermentation enzyme to produce a fermentation mixture;fermenting the fermentation mixture in the organic solvent to producetheaflavins; and separating the theaflavins from the fermentationmixture to produce theaflavin composition.
 22. The method of claim 21wherein the first batch of tea leaves are green tea.
 23. The method ofclaim 21 wherein the ratio of tea leaves to organic solvent is betweenabout 1:10 and about 1:30.
 24. The method of claim 21 wherein extractingpolyphenols from the tea leaves proceeds for about 20 to about 60minutes at between about 25° C. and about 60° C.
 25. The method of claim21 wherein the organic stock substrate solution is concentrated byremoving the organic solvent to yield a solid content of about 0.5% toabout 5% w/v.
 26. The method of claim 21 wherein the second batch of tealeaves are substantially frozen.
 27. The method of claim 21 wherein thefermentation mixture is a ratio of stock substrate solution to stockfermentation enzyme between about 5:1 to about 20:1 (w:w).
 28. Themethod of claim 21 wherein fermentation proceeds between about 4 andabout 8 hours at a stirring speed between about 30 and about 150 rpm andat between about 20° C. and about 40° C.
 29. The method of claim 21wherein oxygen is added to the fermentation mixture during fermentation.30. The method of claim 21 wherein after fermentation, a resultingorganic phase is separated from the fermentation mixture.
 31. The methodof claim 21 wherein water is added to the resulting organic phase in aratio of between about 1:1 and about 1:25 by weight and substantiallyall organic solvent is removed to produce aqueous theaflavin extract.32. The method of claim 21 wherein insoluble impurities are separatedfrom the aqueous theaflavin extract to produce purified aqueoustheaflavin extract.
 33. The method of claim 21 wherein the purifiedaqueous theaflavin extract is lyophilized or spray dried.
 34. The methodof claim 21 wherein the organic solvent is selected from the groupconsisting of methyl acetate, ethyl acetate, propyl acetate andisopropyl acetate.
 35. The method of claim 21 wherein the organicsolvent is selected from the group consisting of ethyl alcohol, propylalcohol, and isopropyl alcohol.
 36. The method of claim 21 wherein theorganic solvent is selected from the group consisting of butanone,diethyl ether, dipropyl ether, and methyl-tert-butyl ether.
 37. Themethod of claim 21 wherein the organic solvent is ethyl acetate.